Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126544041 | 12654404 | 1 | I | 20160519 | 20160520 | 20160816 | 20160816 | PER | US-DRREDDYS-DRL/USA/16/0079987 | DR REDDYS | 68.00 | YR | M | Y | 79.38000 | KG | 20160816 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126544041 | 12654404 | 1 | PS | Levofloxacin Tablets 500 mg | LEVOFLOXACIN | 1 | Oral | U | U | UNKNOWN | 76710 | 500 | MG | TABLET | QD | ||||
| 126544041 | 12654404 | 2 | SS | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | Unknown | U | UNKNOWN | 50564 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126544041 | 12654404 | 1 | Pneumonia |
| 126544041 | 12654404 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126544041 | 12654404 | Diarrhoea | |
| 126544041 | 12654404 | Drug hypersensitivity | |
| 126544041 | 12654404 | Flushing | |
| 126544041 | 12654404 | Peripheral swelling |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126544041 | 12654404 | 1 | 20160518 | 0 |